| Weight | 186.205 g/mol |
|---|---|
| Formula | C5H9F3O2Si |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Trimethylsilyl trifluoroacetate (400-53-3)
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- A novel oxidative azidation of aromatic compounds with hypervalent iodine reagent, phenyliodine(III) bis(trifluoroacetate) (PIFA) and trimethylsilyl azide (Tetrahedron Letters, 1991)
- A Novel and Direct Alkyl Azidation of p-Alkylanisoles Using Phenyl Iodine(III) Bis(trifluoroacetate) (PIFA) and Trimethylsilyl Azide (Synlett, 1994)
- Interaction of bis(trimethylsilyl)acetylene complex of titanocene with mercury trifluoroacetate (Russian Chemical Bulletin, 2003)
- Gas-phase structure, rotational barrier and vibrational properties of trimethylsilyl trifluoroacetate CF3C(O)OSi(CH3)3: An experimental and computational study (Journal of Molecular Structure, 2010)
- ChemInform Abstract: A Novel Oxidative Azidation of Aromatic Compounds with Hypervalent Iodine Reagent, Phenyliodine(III) Bis(trifluoroacetate) (PIFA), and Trimethylsilyl Azide. (ChemInform, 2010)
- ChemInform Abstract: A Novel and Direct Alkyl Azidation of pAlkylanisoles (I) Using Phenyliodine(III) Bis(trifluoroacetate) (PIFA) and Trimethylsilyl Azide. (ChemInform, 2010)
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SMILESC[Si](C)(C)OC(=O)C(F)(F)F
-
InChIKeyVIYXXANHGYSBLY-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
Similar Compounds
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(18306-79-1)
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(454-31-9)
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(406-95-1)
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(1895-39-2)
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(500-73-2)
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(509-09-1)
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1 alternate name
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(1550-44-3)
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(2160-89-6)
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1 alternate name
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(360-34-9)
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Ethyl chlorodifluoroacetate
(383-62-0)
1 alternate name
3 suppliers
Trimethylsilyl trifluoroacetate
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